US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 3, 2014 (12 years ago)

Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, 50 mL Single-dose Flip top Vial…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility; improperly crimped fliptop vials

What was recalled

Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, 50 mL Single-dose Flip top Vial (C-II), Rx only, 25 units per box/50 units per case, Hospira Inc., Lake Forest, IL --- NDC 0409-9094-61

Recalling firm
Hospira Inc.
NDC code
0409-9094-61
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0294-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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